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Clinical Trial Summary

The objective of this prospective, randomized,controlled and multicenter trial is, to compare recurrent-restenosis rates in the balloon expandable VISIO-PRO stent arm and the selfexpandable PROTEGE GPS stent arm 12 month after treatment of stenosis or occlusions of common and external iliac artery disease.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01305174
Study type Interventional
Source Medical Care Center Prof. Mathey, Prof. Schofer, Ltd.
Contact
Status Terminated
Phase Phase 4
Start date October 2010
Completion date July 2014

See also
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Completed NCT01016275 - Misago Iliac Study N/A